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Longitudinal Registry of Endovascular Thoracoabdominal Aneurysms

Longitudinal Registry of Endovascular Thoracoabdominal Aneurysms: Study of Fenestrated and Branched Stent Grafts in the Treatment of Aortic Aneurysms

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03499431
Acronym
LoRETA
Enrollment
1000
Registered
2018-04-17
Start date
2018-04-30
Completion date
2023-03-31
Last updated
2018-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aneurysm, Aortic Aneurysm

Brief summary

The purpose of this study is to evaluate the long-term safety and performance of complex endovascular aneurysm repair by inclusion in a longitudinal registry

Detailed description

This is a Global, multicenter, prospective, observational, non-randomized, single-arm, open clinical study will evaluate the long term (i.e. \>5 years) safety and efficacy of complex endovascular repair This study will enroll all patients treated with Fenestrated and Branched devices in Europe and Canada that follow all inclusion criteria and none of the exclusion criteria. The total duration of the study will be of approximately 7 years.

Interventions

Standard of care, treatment of thoracoabdominal aneurysms using endovascular techiniques.

Sponsors

University Hospital, Lille
CollaboratorOTHER
Skane University Hospital
CollaboratorOTHER
Tara Mastracci
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient eligibility for enrolment shall be based on known information at the time of the procedure. Information obtained at a later date may contradict these criteria, but this will not be considered a deviation of the Study Plan. Inclusion criteria A patient is deemed suitable for inclusion in the study if the patient meets both of the following criteria: 1. Patient requires endovascular repair of a thoracic, thoraco-abdominal or abdominal aortic or aorto-iliac aneurysm having morphology suitable for endovascular repair with complex endograft. 2. Patients (or their legal representative for minor patients) who do not object to (oral non-objection declaration, and signed consent form) collection and transmission of his/her data.

Exclusion criteria

* Patients are excluded from enrolment into the study if any of the following are true: 1. Patients whose imaging follow-up is impossible, i.e. patients who are not able to send their follow up CT scans or Duplex US

Design outcomes

Primary

MeasureTime frameDescription
Longterm Aneurysm Related Mortality7 yearsDeath attributed to aneurysm rupture

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026